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FDA 510(k)

ARTERIOSONDE BLOOD PRESS. MNTR. (#1020)

K-Number: K761057 · 1976-12-09

ApplicantRoche Medical Electronics, Inc.
Decision Date1976-12-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARTERIOSONDE BLOOD PRESS. MNTR. (#1020) is the device name listed in this FDA 510(k) record. The listed applicant is Roche Medical Electronics, Inc.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761057. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIOSONDE BLOOD PRESS. MNTR. (#1020)?

ARTERIOSONDE BLOOD PRESS. MNTR. (#1020) is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Roche Medical Electronics, Inc.. The 510(k) number is K761057.

When did ARTERIOSONDE BLOOD PRESS. MNTR. (#1020) receive FDA 510(k) clearance?

ARTERIOSONDE BLOOD PRESS. MNTR. (#1020) received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761057.

Who is the listed applicant for ARTERIOSONDE BLOOD PRESS. MNTR. (#1020)?

The FDA 510(k) record lists Roche Medical Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTERIOSONDE BLOOD PRESS. MNTR. (#1020)?

The FDA product code for ARTERIOSONDE BLOOD PRESS. MNTR. (#1020) is DXN.

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Related Devices (Code: DXN)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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